Cytoscape Web
Click node...

Autosomal recessive limb-girdle muscular dystrophy type 2D
1 OMIM reference -
1 associated gene
7 connected diseases
No signs/symptoms info
Disease Type of connection
Autosomal recessive limb-girdle muscular dystrophy type 2P
Muscle-eye-brain disease with bilateral multicystic leucodystrophy
Fibronectin glomerulopathy
X-linked dystonia-parkinsonism
Autosomal recessive limb-girdle muscular dystrophy type 2E
Autosomal recessive limb-girdle muscular dystrophy type 2F
Familial isolated dilated cardiomyopathy
Synonym(s):
- Alpha-sarcoglycanopathy
- LGMD2D
- Limb-girdle muscular dystrophy due to alpha-sarcoglycan deficiency
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
SGCA Q16586600119
No signs/symptoms info available.